Inhibition of Vascular Endothelial Growth Factor Receptor 3 Reduces Migration of Gastric Cancer Cells
- Authors
- Lim, Jaeyoung; Ryu, Ji Hyeon; Kim, Eun-Jin; Ham, Songhee; Kang, Dawon
- Issue Date
- 14-Sep-2015
- Publisher
- TAYLOR & FRANCIS INC
- Keywords
- Cell movement; Gastric neoplasms; Vascular endothelial growth factor C; Vascular endothelial growth factor receptor-3
- Citation
- CANCER INVESTIGATION, v.33, no.8, pp.398 - 404
- Indexed
- SCIE
SCOPUS
- Journal Title
- CANCER INVESTIGATION
- Volume
- 33
- Number
- 8
- Start Page
- 398
- End Page
- 404
- URI
- https://scholarworks.bwise.kr/gnu/handle/sw.gnu/17017
- DOI
- 10.3109/07357907.2015.1047509
- ISSN
- 0735-7907
- Abstract
- Angiogenesis induced by proangiogenic molecules such as vascular endothelial growth factor (VEGF) is a key process in the progression and metastasis of gastric cancer. In this study, we investigated the role of VEGF-C/VEGF receptor 3 (VEGFR3) axis in cell proliferation and migration/invasion of human gastric cancer cells (hGCCs). VEGF-C did not enhance cell proliferation but increased cell migration/invasion by approximately approximate to 50% in hGCCs (AGS and SNU-484). MAZ51, a VEGFR3 inhibitor, reduced the VEGF-C-induced increase in migration/invasion by approximate to 30% (p < 0.05). These results suggest that VEGFR3 could be a therapeutic target for reducing the metastasis of gastric cancer cells.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Medicine > Department of Medicine > Journal Articles
![qrcode](https://api.qrserver.com/v1/create-qr-code/?size=55x55&data=https://scholarworks.gnu.ac.kr/handle/sw.gnu/17017)
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.